91 research outputs found

    Metal Recovery from Sludge through the Combination of Hydrothermal Sulfidation and Flotation

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    AbstractThe heavy metal in the waste can react with sulfur and be converted to metal sulfide through the hydrothermal sulfidation. For metal recovery, the synthetic metal sulfide can be enriched through subsequent flotation process. It is a novel way for the recovery of heavy metal from the sludge. In this study, the effects of liquid/solid ratio, mineralizer concentration, precursor concentration and dosage of sulfur on the sulfidation extent and floatation index were investigated. Result shows that with a precursor concentration of 15%, a Zn/S molar ratio of 1:1.2, a liquid/solid ratio of 3:1, the sulfidation extent of zinc in the sludge was greater than 92%, while the flotation recovery of zinc reached up to 45.34%. The toxicity characteristic leaching procedure (TCLP) revealed that stabilization and detoxification of heavy metals occurred during sulfidation

    Ion Bridging by Carbon Dioxide Facilitates Electrochemical Energy Storage at Charged Carbon–Ionic–Liquid Interfaces

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    Abstract Solvent free ionic liquid (IL) electrolytes facilitate high‐voltage supercapacitors with enhanced energy density, but their complex ion arrangement and through that the electrochemical properties, are limited by strong Coulombic ordering in the bulk state and like‐charged ion repulsion at electrified interfaces. Herein, a unique interfacial phenomenon resulting from the presence of carbon dioxide loaded in 1‐Ethyl‐3‐methylimidazoliumtetrafluorborate electrolyte that simultaneously couples to IL ions and nitrogen‐doped carbonaceous electrode is reported. The adsorbed CO 2 molecule polarizes and mitigates the electrostatic repulsion among like‐charged ions near the electrified interface, leading to an ion “bridge effect” with increased interfacial ionic density and significantly enhanced charge storage capability. The unpolarized CO 2 possessing a large quadrupole moment further reduces ion coupling, resulting in higher conductivity of the bulk IL and improved rate capability of the supercapacitor. This work demonstrates polarization‐controlled like‐charge attraction at IL–electrode–gas three‐phase boundaries, providing insights into manipulating complex interfacial ion ordering with small polar molecule mediators.Solvent‐free ionic liquid (IL) electrolytes enable high‐voltage and high‐energy‐density applications. The proposed bridge effect with CO 2 loaded in an IL electrolyte acting as a mediator on the nitrogen‐doped electrode surface, alleviates the undesired Coulombic ordering and interfacial like‐charged ion repulsion. By breaking the limitation of interfacial ion packing density, this effect results in a significant enhancement of charge storage capability. imag

    Preparation of Antibacterial Color-Coated Steel Sheets

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    A simple method to fabricate antibacterial color-coated steel sheet was presented. The Ag-loaded TiO2 was well dispersed in steel coil coating coupled with some special additives, such as plasticizer, wetting dispersant, and flow agent, and finally became the part of coil coating without any negative influence on the properties of final products. The best process parameters were obtained by substantive trial experiments. Ag-loaded TiO2 with the addition of 2% (w/w) in steel coil coating not only improved antibacterial efficiency of the antibacterial color-coated sheet by reaching 99.99%, but also greatly increased the degradation percentage of methyl orange to 88% without decreasing physical properties. The antibacterial color-coated sheets are expected to be used as antimicrobial products in the construction industry considering its low cost and high effectiveness in inhibiting the growth of bacteria

    Heteroatoms Induce Localization of the Electric Field and Promote a Wide Potential-Window Selectivity Towards CO in the CO2 Electroreduction

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    Carbon dioxide electroreduction (CO2RR) is a sustainable way of producing carbon-neutral fuels. Product selectivity in CO2RR is regulated by the adsorption energy of reaction-intermediates. Here, we employ differential phase contrast-scanning transmission electron microscopy (DPC-STEM) to demonstrate that Sn heteroatoms on a Ag catalyst generate very strong and atomically localized electric fields. In situ attenuated total reflection infrared spectroscopy (ATR-IR) results verified that the localized electric field enhances the adsorption of *COOH, thus favoring the production of CO during CO2RR. The Ag/Sn catalyst exhibits an approximately 100 % CO selectivity at a very wide range of potentials (from -0.5 to -1.1 V, versus reversible hydrogen electrode), and with a remarkably high energy efficiency (EE) of 76.1 %

    Two-Dimensional Titanium Carbides (Ti3C2Tx) Functionalized by Poly(m-phenylenediamine) for Efficient Adsorption and Reduction of Hexavalent Chromium

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    Titanium carbides (MXenes) are promising multifunctional materials. However, the negative surface charge and layer-by-layer restacking of MXenes severely restrict their application in the field of anionic pollutants, including in hexavalent chromium (Cr(VI)). Herein, Ti3C2Tx MXenes was functionalized through in situ polymerization and intercalation of poly(m-phenylenediamine) (PmPD), then Ti3C2Tx/PmPD composites were obtained. Delightedly, Ti3C2Tx/PmPD composites exhibited positive surface charge, expanded interlayer spacing, and enhanced hydrophobicity. Furthermore, the specific surface area of Ti3C2Tx/PmPD composite was five and 23 times that of Ti3C2Tx and PmPD, respectively. These advantages endowed Ti3C2Tx/PmPD composite with an excellent adsorption capacity of Cr(VI) (540.47 mg g−1), which was superior to PmPD (384.73 mg g−1), Ti3C2Tx MXene (137.45 mg g−1), and the reported MXene-based adsorbents. The Cr(VI) removal mechanism mainly involved electrostatic adsorption, reduction, and chelation interaction. This study developed a simple functionalization strategy, which would greatly explore the potential of MXenes in the field of anionic pollutants

    Numerical Study of Ground Vibrations Caused by Cylindrical Wave Propagation in a Rock Mass with a Structural Plane

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    Stress wave which is caused either by an explosion in a borehole or by an accidental explosion in a tunnel is supposed to be considered under certain circumstances when it propagates through the surrounding rock masses which contain holes in cylindrical form. Studying the ground motion induced by the cylindrical wave propagation is of practical significance for underground rock engineering and underground energy exploitation. The current study presents a numerical study on the ground motion caused by cylindrical P-wave propagation across a rock mass with a structural plane using a discrete element numerical method, UDEC. Firstly, the accuracy and validity of the cylindrical wave propagation simulation in UDEC and of the induced ground vibration are confirmed by comparison with the theoretical results for a special case that there is no structural plane in a rock mass. Secondly, cylindrical wave propagation across a rock mass with a structural plane is simulated, and then, the particle velocity on the ground surface is subsequently obtained. Finally, parametric researches are carried out on the influence of the monitoring point’s position, the structural plane stiffness, and the frequency of incident wave on the peak particle velocities (PPVs) of the ground vibrations

    A series piezoelectric quartz crystal response model for ferrous ion oxidation in the presence of <i>T. ferrooxdians</i>

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    939-942A novel and simple method, series piezoelectric quartz crystal (SPQC) has been used to monitor ferrous ion oxidation in the presence of T. ferrooxidans. By combination of a general SPQC response model with the kinetics of the bacterial growth, a SPQC response model for ferrous ion oxidation in the presence of T.ferrooxidans has been built. The response model can describe the bacterial growth process well. Some important kinetic parameters, such as μm (the maximum specific growth rate of bacterium), K (saturation constant, i.e., the ferrous iron concentration at which the half-maximal growth rate occurs), X0 / Y (ratio of initial bacterial concentration to cell yield coefficient), have been obtained by fitting the model to the experimental curves
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